Indicator for probable inheritance of genetic disease

ABSTRACT

Systems, methods and computer-readable media are provided for identification of patients or family member having genetic disease or probable genetic disease. During or after registration of a patient, parents, grandparents, or siblings of the patient are identified. If it is determined that one of the patient or the parents, grandparents, or siblings of the patient has been assigned with a diagnosis indicating a genetic disease, an alert for genetic disease or probable genetic disease for the patient or family member of the patient is provided. A clinician is then prompted to confirm or rule out the patient or family member inheriting the disease.

BACKGROUND

Many diseases can be passed along from one family member to another.These diseases are often due to changes or mutations in a gene that isinherited from one or both parents. However, these diseases are oftenmisdiagnosed due to incomplete medical records or a lack of knowledge bya patient that a possible genetic disease may have been passed to thepatient. As a result, the opportunity for early diagnosis and treatmentmay be missed and the health of the patient may deteriorate.

SUMMARY

Systems, methods and computer-readable media are provided for theidentification of patients having a probable inheritance of a geneticdisease. In particular, embodiments of the invention are directed toidentifying parents, grandparents, or siblings of a patient collectedduring registration of the patient. If it is determined that one of thepatient or the parents, grandparents, or siblings of the patient hasbeen assigned with a diagnosis indicating a genetic disease, an alertfor a genetic disease or probable genetic disease for patient or familymember of the patient is provided. The alert includes providing agenetic disease or probable genetic disease icon in an electronic healthrecord of the patient or family member of the patient.

In some embodiments, a clinician is prompted to confirm or rule out thepatient or the parents, grandparents, or siblings of the patient havingthe genetic disease. Upon receiving an indication that the patient orfamily member has been ruled out as having the genetic disease, a recordof the patient or family member in the healthcare system is updated withno alerts indicating the patient or family member of the patient doesnot have genetic disease or probable genetic disease. This includesremoving the genetic disease icon or probable genetic disease icon fromthe electronic health record of the patient or family member of thepatient. In contrast, upon receiving an indication that the patient orfamily member has been confirmed as having the genetic disease, theprobable genetic disease icon is replaced with a genetic disease icon inthe electronic health record of the patient or family member indicatingthe patient or family member has the genetic disease.

In this way, embodiments of the invention facilitate the early diagnosisand treatment of genetic diseases.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention is described in detail below with reference to theattached drawing figures, wherein:

FIG. 1 is a block diagram of an exemplary computing environment suitablefor use in implementing the present invention;

FIG. 2 is a block diagram of an exemplary system for the identificationof patients having a probable inheritance of a genetic disease, inaccordance with an embodiment of the present invention;

FIG. 3 is a flow diagram showing an exemplary method of identifyingnewly registered patients having a probable inheritance of a geneticdisease, in accordance with various embodiments of the presentinvention;

FIG. 4 is a flow diagram showing an exemplary method of identifyingalready registered patients having a probable inheritance of a geneticdisease, in accordance with various embodiments of the presentinvention; and

FIGS. 5-12 are exemplary graphical user interfaces illustratingidentification of patients having genetic disease and family member ofthe patient with probable genetic disease, in accordance withembodiments of the present invention.

DETAILED DESCRIPTION

The subject matter of the present invention is described withspecificity herein to meet statutory requirements. However, thedescription itself is not intended to limit the scope of this patent.Rather, the inventors have contemplated that the claimed subject mattermight also be embodied in other ways, to include different steps orcombinations of steps similar to the ones described in this document, inconjunction with other present or future technologies. Moreover,although the terms “step” and/or “block” may be used herein to connotedifferent components of methods employed, the terms should not beinterpreted as implying any particular order among or between varioussteps herein disclosed unless and except when the order of individualsteps is explicitly described.

As noted in the Background, many diseases can be passed along from onefamily member to another. These diseases are often due to changes ormutations in a gene that is inherited from one or both parents. However,these diseases are often misdiagnosed due to incomplete medical recordsor a lack of knowledge by a patient that a possible genetic disease mayhave been passed to the patient. As a result, the opportunity for earlydiagnosis and treatment may be missed and the health of the patient maydeteriorate.

Embodiments of the present invention enable the identification ofpatients or family member having genetic disease or probable geneticdisease. In particular, embodiments of the invention are directed toidentifying parents, grandparents, or siblings of a patient collectedduring registration of the patient. If it is determined that one of thepatient or the parents, grandparents, or siblings of the patient hasbeen assigned with a diagnosis indicating a genetic disease, an alertfor a genetic disease or probable genetic disease for the patient orfamily member of the patient is provided. The alert includes providing agenetic disease icon or or probable genetic icon in an electronic healthrecord of the patient or family member of the patient.

In some embodiments, a clinician is prompted to confirm or rule out thepatient or the parents, grandparents, or siblings of the patient havingthe genetic disease. Upon receiving an indication that the patient orfamily member has been ruled out as having the genetic disease, a recordof the patient or family member in the healthcare system is updated withno alerts indicating the patient or family member does not have geneticdisease or probable genetic disease. This includes removing geneticdisease icon or probable genetic disease icon from the electronic healthrecord of the patient or the family member of the patient. In contrast,upon receiving an indication that the patient or family member has beenconfirmed as having the genetic disease, the probable genetic diseaseicon is replaced with a genetic disease icon in the electronic healthrecord of the patient or family member indicating the patient or familymember has the genetic disease.

In this way, embodiments of the invention facilitate the early diagnosisand treatment of genetic diseases.

Accordingly, in one aspect, an embodiment of the present invention isdirected to one or more computer storage media havingcomputer-executable instructions embodied thereon, that when executed,perform a method for providing an indicator for genetic disease orindicator for probable genetic disease. The method comprises registeringa patient in a healthcare system. The method also comprises receiving aselection of one or more family members comprising parents,grandparents, or siblings of the patient. The method further comprisesdetermining whether any of the one or more family members has beenassigned with a diagnosis indicating a genetic disease.

In another aspect of the invention, an embodiment is directed to one ormore computer storage media having computer-executable instructionsembodied thereon, that when executed, perform a method for providing anindicator for genetic disease or indicator for probable genetic disease.The method comprises identifying parents, grandparents, or siblings of apatient collected during registration of the patient. The method furthercomprises determining that one of the patient or the parents,grandparents, or siblings of the patient has been assigned with adiagnosis indicating a genetic disease. The method also comprisesproviding an alert for genetic disease or an alert for probable geneticdisease for the patient or family member of the patient. The alertincludes providing a genetic disease icon or probable genetic diseaseicon in an electronic health record of the patient or the family memberof the patient.

In a further aspect, an embodiment is directed to a system in ahealthcare computing environment that enables providing an indicator forgenetic disease and indicator for probable genetic disease. The systemcomprises a processor; and a non-transitory computer storage mediumstoring computer-useable instructions that, when used by the processor,cause the processor to: identify parents, grandparents, or siblings of apatient collected during registration of the patient; determine that oneof the patient or the parents, grandparents, or siblings of the patienthas been assigned with a diagnosis indicating a genetic disease; providean alert for genetic disease or alert for probable genetic disease forthe patient or the family member of the patient; and prompt a clinicianto confirm or rule out the patient or family member inheriting thedisease.

An exemplary computing environment suitable for use in implementingembodiments of the present invention is described below. FIG. 1 is anexemplary computing environment (e.g., medical-informationcomputing-system environment) with which embodiments of the presentinvention may be implemented. The computing environment is illustratedand designated generally as reference numeral 100. The computingenvironment 100 is merely an example of one suitable computingenvironment and is not intended to suggest any limitation as to thescope of use or functionality of the invention. Neither should thecomputing environment 100 be interpreted as having any dependency orrequirement relating to any single component or combination ofcomponents illustrated therein.

The present invention might be operational with numerous other purposecomputing system environments or configurations. Examples of well-knowncomputing systems, environments, and/or configurations that might besuitable for use with the present invention include personal computers,server computers, hand-held or laptop devices, wearable devices,multiprocessor systems, microprocessor-based systems, set top boxes,programmable consumer electronics, network PCs, minicomputers, mainframecomputers, distributed computing environments that include any of theabove-mentioned systems or devices, and the like.

The present invention might be described in the general context ofcomputer-executable instructions, such as program modules, beingexecuted by a computer. Exemplary program modules comprise routines,programs, objects, components, and data structures that performparticular tasks or implement particular abstract data types. Thepresent invention might be practiced in distributed computingenvironments where tasks are performed by remote processing devices thatare linked through a communications network. In a distributed computingenvironment, program modules might be located in association with localand/or remote computer storage media (e.g., memory storage devices).

With continued reference to FIG. 1, the computing environment 100comprises a computing device in the form of a control server 102.Exemplary components of the control server 102 comprise a processingunit, internal system memory, and a suitable system bus for couplingvarious system components, including data store 104, with the controlserver 102. The system bus might be any of several types of busstructures, including a memory bus or memory controller, a peripheralbus, and a local bus, using any of a variety of bus architectures.Exemplary architectures comprise Industry Standard Architecture (ISA)bus, Micro Channel Architecture (MCA) bus, Enhanced ISA (EISA) bus,Video Electronic Standards Association (VESA) local bus, and PeripheralComponent Interconnect (PCI) bus, also known as Mezzanine bus.

The control server 102 typically includes therein, or has access to, avariety of computer-readable media. Computer-readable media can be anyavailable media that might be accessed by control server 102, andincludes volatile and nonvolatile media, as well as, removable andnonremovable media. By way of example, and not limitation,computer-readable media may comprise computer storage media andcommunication media. Computer storage media includes both volatile andnonvolatile, removable and non-removable media implemented in any methodor technology for storage of information such as computer-readableinstructions, data structures, program modules or other data. Computerstorage media includes, but is not limited to, RAM, ROM, EEPROM, flashmemory or other memory technology, CD-ROM, digital versatile disks (DVD)or other optical disk storage, magnetic cassettes, magnetic tape,magnetic disk storage or other magnetic storage devices, or any othermedium which can be used to store the desired information and which canbe accessed by control server 102. Computer storage media does notcomprise signals per se. Communication media typically embodiescomputer-readable instructions, data structures, program modules orother data in a modulated data signal such as a carrier wave or othertransport mechanism and includes any information delivery media. Theterm “modulated data signal” means a signal that has one or more of itscharacteristics set or changed in such a manner as to encode informationin the signal. By way of example, and not limitation, communicationmedia includes wired media such as a wired network or direct-wiredconnection, and wireless media such as acoustic, RF, infrared and otherwireless media. Combinations of any of the above should also be includedwithin the scope of computer-readable media.

The control server 102 might operate in a computer network 106 usinglogical connections to one or more remote computers 108. Remotecomputers 108 might be located at a variety of locations in a medical orresearch environment, including clinical laboratories (e.g., moleculardiagnostic laboratories), hospitals and other inpatient settings,ambulatory settings, medical billing and financial offices, hospitaladministration settings, home healthcare environments, clinicians'offices, Center for Disease Control, Centers for Medicare & MedicaidServices, World Health Organization, any governing body either foreignor domestic, Health Information Exchange, and any healthcare/governmentregulatory bodies not otherwise mentioned. Clinicians may comprise atreating physician or physicians; specialists such as intensivists,surgeons, radiologists, cardiologists, and oncologists; emergencymedical technicians; physicians' assistants; nurse practitioners;nurses; nurses' aides; pharmacists; dieticians; microbiologists;laboratory experts; laboratory technologists; genetic counselors;researchers; students; and the like. The remote computers 108 might alsobe physically located in nontraditional medical care environments sothat the entire healthcare community might be capable of integration onthe network. The remote computers 108 might be personal computers,servers, routers, network PCs, peer devices, other common network nodes,or the like and might comprise some or all of the elements describedabove in relation to the control server 102. The devices can be personaldigital assistants or other like devices.

Computer networks 106 comprise local area networks (LANs) and/or widearea networks (WANs). Such networking environments are commonplace inoffices, enterprise-wide computer networks, intranets, and the Internet.When utilized in a WAN networking environment, the control server 102might comprise a modem or other means for establishing communicationsover the WAN, such as the Internet. In a networking environment, programmodules or portions thereof might be stored in association with thecontrol server 102, the data store 104, or any of the remote computers108. For example, various application programs may reside on the memoryassociated with any one or more of the remote computers 108. It will beappreciated by those of ordinary skill in the art that the networkconnections shown are exemplary and other means of establishing acommunications link between the computers (e.g., control server 102 andremote computers 108) might be utilized.

In operation, an organization might enter commands and information intothe control server 102 or convey the commands and information to thecontrol server 102 via one or more of the remote computers 108 throughinput devices, such as a keyboard, a pointing device (commonly referredto as a mouse), a trackball, or a touch pad. Other input devicescomprise microphones, satellite dishes, scanners, or the like. Commandsand information might also be sent directly from a remote healthcaredevice to the control server 102. In addition to a monitor, the controlserver 102 and/or remote computers 108 might comprise other peripheraloutput devices, such as speakers and a printer.

Although many other internal components of the control server 102 andthe remote computers 108 are not shown, such components and theirinterconnection are well known. Accordingly, additional detailsconcerning the internal construction of the control server 102 and theremote computers 108 are not further disclosed herein.

Turning now to FIG. 2, an exemplary computing system environment 200 isdepicted suitable for use in implementing embodiments of the presentinvention. The computing system environment 200 is merely an example ofone suitable computing system environment and is not intended to suggestany limitation as to the scope of use or functionality of embodiments ofthe present invention. Neither should the computing system environment200 be interpreted as having any dependency or requirement related toany single module/component or combination of modules/componentsillustrated therein.

The computing system environment 200 includes a clinician device 210, agenetic disease engine 212, healthcare system 214, and electronic healthrecord(s) (EHRs) 216 a-216 n, all in communication with one another viaa network (not shown in FIG. 2). The network may include, withoutlimitation, one or more secure local area networks (LANs) or wide areanetworks (WANs). The network may be a secure network associated with afacility such as a healthcare facility. The secure network may requirethat a user log in and be authenticated in order to send and/or receiveinformation over the network.

In some embodiments, one or more of the illustrated components/modulesmay be implemented as stand-alone applications. In other embodiments,one or more of the illustrated components/modules may be distributedacross multiple genetic disease engines. The components/modulesillustrated in FIG. 2 are exemplary in nature and in number and shouldnot be construed as limiting. Any number of components/modules may beemployed to achieve the desired functionality within the scope ofembodiments hereof. Further, components/modules may be located on anynumber of servers. By way of example only, the genetic disease engine212 might reside on a server, cluster of servers, or a computing deviceremote from one or more of the remaining components.

It should be understood that this and other arrangements describedherein are set forth only as examples. Other arrangements and elements(e.g., machines, interfaces, functions, orders, and groupings offunctions, etc.) can be used in addition to or instead of those shown,and some elements may be omitted altogether. Further, many of theelements described herein are functional entities that may beimplemented as discrete or distributed components or in conjunction withother components/modules, and in any suitable combination and location.Various functions described herein as being performed by one or moreentities may be carried out by hardware, firmware, and/or software. Forinstance, various functions may be carried out by a processor executinginstructions stored in memory.

Each of the EHRs 216 a-216 n is configured to provide information to andstore information communicated by, for example, the genetic diseaseengine 212 or healthcare system 214. The information stored inassociation with the EHRs 216 a-216 n may comprise information receivedfrom or used by various components of the genetic disease engine 212 orhealthcare system 214. As illustrated in FIG. 2, it is contemplated thatmultiple EHRs 216 a-216 n may be utilized by the present invention. Inthis way data and context may be aggregated from multiple sources (e.g.,EHRs) or multiple locations.

EHRs 216 a-216 n may include information corresponding to patientsassociated with one or more healthcare facilities. EHRs 216 a-216 n maycomprise electronic clinical documents such as images, clinical notes,orders, summaries, reports, analyses, information received from thegenetic disease engine 212, healthcare system 214, and medical devices(not shown in FIG. 2), or other types of electronic medicaldocumentation relevant to a particular patient's condition and/ortreatment. Electronic clinical documents contain various types ofinformation relevant to the condition and/or treatment of a particularpatient and can include information relating to, for example, patientidentification information, images, alert history, culture results,physical examinations, vital signs, past medical histories, surgicalhistories, family histories, histories of present illnesses, current andpast medications, allergies, symptoms, past orders, completed orders,pending orders, tasks, lab results, other test results, patientencounters and/or visits, immunizations, physician comments, nursecomments, other caretaker comments, clinician assignments, and a host ofother relevant clinical information.

The content and volume of such information in the EHRs 216 a-216 n isnot intended to limit the scope of embodiments of the present inventionin any way. Further, though each EHRs 216 a-216 n is illustrated as asingle, independent component, the EHRs 216 a-216 n may, in fact,include a plurality of applications and/or storage devices, forinstance, a database cluster.

The clinician device 210 may be any type of computing device capable ofcommunicating with the genetic disease engine 212 or healthcare system214 to interact with documentation stored in the EHRs 216 a-216 n. Suchdevices may include any type of mobile and portable devices includingcellular telephones, personal digital assistants, tablet PCs, smartphones, and the like.

Genetic disease engine 212 may include a processing unit, internalsystem memory, and a suitable system bus for coupling various systemcomponents, including one or more data stores for storing information(e.g., files and metadata associated therewith). The genetic diseaseengine 212 typically includes, or has access to, a variety ofcomputer-readable media.

The computing system environment 200 is merely exemplary. While thegenetic disease engine 212 is illustrated as a single unit, it will beappreciated that the genetic disease engine 212 is scalable. Forexample, the genetic disease engine 212 may in actuality include aplurality of computing devices in communication with one another. Thesingle unit depictions are meant for clarity, not to limit the scope ofembodiments in any form.

Initially, a clinician registers a patient in healthcare system 214,such as by using clinician device 210. In some embodiments, the patientmay already be registered in healthcare system 214. The clinician mayutilize the clinician device 210 to access the genetic disease engine212 to identify parents, grandparents, or siblings of that patient. Suchrelationships may have been collected during registration of thepatient.

The genetic disease engine 212 may determine, such as by accessingEHR(s) 216 a-216 n for each of the patient and/or identified relativesof the patient, that one of the patient or the parents, grandparents, orsiblings of the patient has been assigned with a diagnosis indicating agenetic disease. The genetic disease engine 212 may additionally providean alert for genetic disease or probable genetic disease for the patientor family member of the patient. The alert includes providing a geneticdisease icon and/or probable genetic disease icon, such as in the EHR ofthe patient or family member. The probable genetic disease icon enablesa clinician to quickly identify which patients may be at risk for havinga genetic disease. Interaction with the probable genetic disease iconprovides additional information such as information about other familymembers corresponding to the genetic disease (e.g., a relative name,relationship to the patient, and diagnosis). Further, the geneticdisease engine 212 may prompt the clinician to confirm or rule out thepatient or family member having the disease.

In some embodiments, the genetic disease engine 212 may communicateorders that assist in confirming or ruling out the patient or familymember having the disease. For example, the genetic disease engine 212may communicate with a laboratory to order a test that may confirm orrule out the patient or family member having the disease. The geneticdisease engine 212 may also communicate with one or more medical devicesthat may provide insight into whether the patient or family member hasthe disease. Further, the genetic disease engine 212 may communicate anorder to a pharmacy system to order a medication that may prevent orlessen the risk or symptoms of the genetic disease should the patient orfamily member be confirmed as having the genetic disease. Still further,the genetic disease engine 212 may communicate information regarding thegenetic disease to the clinician, the patient or family member, or toothers authorized to have such information.

In some embodiments, upon receiving an indication that the one or morefamily members was misdiagnosed with a genetic disease, the records forthe patient and corresponding family members are updated in thehealthcare system with no alerts. This indicates that the patient andthe corresponding family members do not have a probable genetic disease.

In some embodiments, upon receiving an indication that the patient hasbeen ruled out as having the genetic disease, the records for thepatient or family member is updated in the healthcare system with noalerts. This also indicates the patient does not have a probable geneticdisease. Additionally, the probable genetic disease icon is removed fromthe electronic health record of the patient or family member of thepatient.

In some embodiments, upon receiving an indication that the patient hasbeen confirmed as having the genetic disease, the probable geneticdisease icon is replaced with a genetic disease icon in the electronichealth record of the patient. This indicates the patient has the geneticdisease.

Turning now to FIG. 3, a flow diagram is provided illustrating a method300 of identifying patients having a probable inheritance of a geneticdisease, in accordance with an embodiment of the present invention.Initially, as shown at step 310, a patient is registered in a healthcaresystem, such as by using by using clinician device 210 of FIG. 2.

At step 312, a selection of one or more family members comprisingparents, grandparents, or siblings of the patient is received. Forexample, during registration, the patient may have identified one ormore family members that have already been registered in healthcaresystem. Or, the patient may have already been identified by anotherfamily member when that family member was registered in the healthcaresystem. If the patient does not have any identified family members, thepatient is registered in the healthcare system, at step 316, with noalerts for a possible genetic disease. This indicates the patient doesnot have a probable genetic disease.

At step 314, if the patient has identified family members, it isdetermined whether any of the family members has been assigned with adiagnosis indicating a genetic disease. In embodiments, if a familymember has not been assigned with a diagnosis indication a geneticdisease, the patient is registered in the healthcare system, at step316, with no alerts for a possible genetic disease. This indicates thepatient does not have a probable genetic disease.

In embodiments, if a family member has been assigned with a diagnosisindication a genetic disease, an alert is provided in the healthcaresystem, at step 318, indicating the patient has a probable geneticdisease. The alert includes providing a probable genetic disease icon inan EHR of the patient. A genetic disease icon may be provided for theone or more family members that has previously been assigned with adiagnosis indicating a genetic disease. In some embodiments, the alertincludes an option to assign the genetic disease to the patient or otherfamily members within the healthcare system.

Also, at step 314, if the If the patient does not have any identifiedfamily members, the patient is registered in the healthcare system, atstep 316, with no alerts for a possible genetic disease. This indicatesthe patient does not have a probable genetic disease.

If an interaction with the genetic disease icon is received, a relativename, relationship to the patient, and diagnosis may be provided. Thisenables the clinician how to proceed to determine how to confirm or ruleout the possibility of the patient having the genetic disease. In someembodiments, the clinician is prompted to do so.

Upon receiving an indication that the one or more family members wasmisdiagnosed with a genetic disease, records for the patient andcorresponding family members may be updated in the healthcare systemwith no alerts. Any related probable genetic disease icons are removedfor the appropriate EHRs. This indicates the patient and thecorresponding family members do not have a probable genetic disease.

In some embodiments, if an indication is received that the patient hasbeen ruled out as having the genetic disease, the record for the patientis updated in the healthcare system with no alerts. This indicatesindicating the patient does not have the genetic disease, which includesremoving the probable genetic disease icon from the EHR of the patient.In contrast, in some embodiments, if an indication is received that thepatient has been confirmed as having the genetic disease, the probablegenetic disease icon is replaced with a genetic disease icon in the EHRof the patient indicating the patient has the genetic disease.

Referring now to FIG. 4, a flow diagram is provided illustrating amethod 400 of providing an indicator for probable inheritance of geneticdisease, in accordance with an embodiment of the present invention.Initially, in some embodiments and as shown at step 410, a patient isalready registered in the healthcare system. Parents, grandparents, orsiblings of the patient that were collected during registration of thepatient are identified, at step 412, such as by receiving a selection ofthe parents, grandparents, or siblings of the patient via a cliniciandevice. If no relatives are selected, no alerts for possible geneticdisease are provided, as shown at step 416.

At step 414, if it is determined that one of the patient or the parents,grandparents, or siblings of the patient has not been assigned with adiagnosis indicating a genetic disease, no alerts for possible geneticdisease are provided, as shown at step 416. However, if it is determinedthat one of the patient or the parents, grandparents, or siblings of thepatient has been assigned with a diagnosis indicating a genetic disease,an alert for possible genetic disease for the patient or family memberof the patient is provided at step 418. The clinician may be prompted toconfirm or rule out the patient as having the disease.

In embodiments, the alert includes an option to assign the patient orother family member as having the genetic disease within the healthcaresystem. For those family members that have been assigned as having thegenetic disease, a genetic disease icon may be provided in theirrespective EHRs. When an interaction with the genetic disease icon isreceived, a relative name, relationship to the patient, and diagnosis isprovided.

In some embodiments, if an indication is received that the patient orfamily member has been ruled out as having the genetic disease, a recordof the patient or family member may be updated in the healthcare systemwith no alerts. This indicates the patient or family member does nothave genetic disease or probable genetic disease and may includeremoving the genetic disease icon or probable genetic disease icon fromthe EHR of the patient or family member of the patient.

In some embodiments, if an indication is received that the patient orfamily member has been confirmed as having the genetic disease, theprobable genetic disease icon may be replaced with a genetic diseaseicon in the electronic health record of the patient or family memberindicating the patient or family member has the genetic disease.

Turning now to FIGS. 5-12, graphical user interfaces (GUIs) illustratingidentification of patients having genetic disease and family member ofthe patient with probable genetic disease, in accordance withembodiments of the present invention are provided. GUI 500 enables auser to associate a diagnosis 502 (such as via clinician device 210 ofFIG. 2) with a patient. If the diagnosis is a genetic disease, thegenetic disease box 504 may be selected. Once these selections aresaved, the system considers the diagnosis associated with the patient agenetic disease.

In FIG. 6, graphical user interface 600 illustrates the system providinga genetic disease icon 602 for the patient. The genetic disease icon 602indicates that the patient has been diagnosed with a genetic disease. Anew column 604 called “Genetic Disease” may also added that displays theicon for the corresponding diagnosis associated with the patient. Asshown by graphical user interface 700 in FIG. 7, upon hovering overeither icon 702, details 704 regarding the genetic disease are provided.For example, the details 704 may include patient name, relationship tothe patient, and diagnosis.

As shown in FIG. 8, graphical user interface 800 illustrates a patient802 being registered for the first time in the healthcare system. Thesystem determines if any relationships between the newly registeredpatient and existing patients are identified within the system. Forexample, if during registration, a relative is selected as having arelationship to the patient 802, and that relative is already associatedwith a diagnosis that has been marked as a genetic disease, a probablegenetic disease icon 804 is displayed for patient 802. The probablygenetic disease icon suggests that the patient 802 may have thepossibility of inheriting the same genetic disease as the relative. Thisenables the clinician to take appropriate measures to confirm thediagnosis or rule out the possibility of inheriting the disease.

FIG. 9 depicts graphical user interface 900 illustrating a savedrelationship between the newly registered patient 902 and an existentpatient 912. Since the existing patient 904 is associated with adiagnosis 914 which is marked as a genetic disease, the system displaysa probable genetic disease icon 908 for the newly registered patient902. This indicates the possibility of inheriting a genetic disease. Inthis way, the system identifies relationships that have been establishedand assigns probable genetic disease icons for newly registered patientsas appropriate. As shown, upon interacting with the probable geneticdisease icon 908, details 910 regarding the genetic disease areprovided. As illustrated, the details 910 may include patient name,relationship to the patient, and diagnosis.

Turning now to FIG. 10, graphical user interface 1000 illustrates whathappens after the newly registered patient 1014 has been identified as arelative of the patient 1002 having the genetic disease. Uponinteracting with the genetic disease icon 1004, details 1010 regardingthe genetic disease are provided. As illustrated, the details 1010 mayinclude patient name, relationship to the patient, and diagnosis.

In FIG. 11, graphical user interfaces 1100, 1110, 1120 illustratespatients (i.e., Patient1 and Patient2) having an existing relationshipand already being registered in the healthcare system. Based on therelationship established between Patient1 and Patient 2, the systemrecognizes that if one of the patients is diagnosed with a geneticdisease at any point in time, the related patient will have thepossibility of inheriting the genetic disease.

For example, suppose a diagnosis 1102 is added for Patient1. If thatdiagnosis is not marked as a genetic disease in the genetic disease box1104, the system will not display the genetic disease icon for Patient1or the probable genetic disease icon for Patient2. However, if at alater point in time, and referring to FIG. 12, graphical user interfaces1200, 1210, 1220 illustrates a scenario where the clinician marks thediagnosis 1202 associated with Patient1 as a genetic disease in thegenetic disease box 1204. In this case, the system displays the geneticdisease icon 1212 for Patient1 and the probable genetic disease icon1222 for Patient2. Upon interacting with the genetic disease icon 1212or probable genetic disease icon 1222, details 1214 or details 1224regarding the genetic disease are provided. As illustrated, the details1214, 1224 may include patient name, relationship to the patient, anddiagnosis

In various embodiments, the system may correct a misdiagnosis ormistake. For example, if a diagnosis should not have marked as a geneticdisease in the genetic disease box or was marked by mistake, thediagnosis can be unmarked as a genetic disease by unchecking the geneticdisease box. As a result, the genetic disease icon for the patient andthe probable genetic disease icon for the relative are removed uponsaving the correction and no icons are provided.

As can be understood, the present invention provides systems, methods,and user interfaces for providing real-time analysis and annotation ofclinical documents in a distributed system. The present invention hasbeen described in relation to particular embodiments, which are intendedin all respects to be illustrative rather than restrictive. Alternativeembodiments will become apparent to those of ordinary skill in the artto which the present invention pertains without departing from itsscope.

From the foregoing, it will be seen that this invention is one welladapted to attain all the ends and objects set forth above, togetherwith other advantages which are obvious and inherent to the system andmethod. It will be understood that certain features and subcombinationsare of utility and may be employed without reference to other featuresand subcombinations. This is contemplated and within the scope of theclaims.

What is claimed is:
 1. Computer-readable media havingcomputer-executable instructions embodied thereon that when executed,facilitate a method for providing an indicator for genetic disease andprobable genetic disease, the method comprising: registering, via aclinician device, a patient in a healthcare system; accessing, via theclinician device, a genetic disease engine to identify parents,grandparents, or siblings, of the patient; receiving, at the cliniciandevice, a selection of one or more family members of the parents,grandparents, or siblings of the patient; and determining, at thegenetic disease engine by communicating with one or more medical devicesthat provide insight into whether any of the one or more family membershas been assigned with a diagnosis indicating a genetic disease, whetherany of the one or more family members has been assigned with thediagnosis indicating the genetic disease; upon determining a familymember of the one or more family members has been assigned with thediagnosis indicating the genetic disease, providing, by the geneticdisease engine, an alert in the healthcare system indicating the patienthas a probable genetic disease, the alert including providing a probablegenetic disease icon in an electronic health record of the patient;communicating, by the genetic disease engine, orders that assist inconfirming or ruling out the patient having the disease; prompting aclinician, via the clinician device, to confirm or rule out the patienthaving the disease; and upon receiving an indication that the patient orfamily member has been confirmed as having the genetic disease,replacing the probable genetic disease icon with a genetic disease iconin the electronic health record of the patient or family memberindicating the patient or family member has the genetic disease.
 2. Thecomputer-readable media of claim 1, wherein the alert includes an optionto assign the genetic disease to the patient or other family memberswithin the healthcare system.
 3. The computer-readable media of claim 1,further comprising if any of the one or more family members has not beenassigned with a diagnosis indicating a genetic disease, registering thepatient in the healthcare system with no alerts indicating the patientdoes not have a probable genetic disease.
 4. The computer-readable mediaof claim 2, further comprising providing a genetic disease icon for theone or more family members that has been assigned with a diagnosisindicating a genetic disease.
 5. The computer-readable media of claim 4,further comprising receiving an interaction with the genetic diseaseicon.
 6. The computer-readable media of claim 5, further comprising,upon receiving the interaction with the genetic disease icon, providinga relative name, relationship to the patient, and diagnosis.
 7. Thecomputer-readable media of claim 1, further comprising providing aprobable genetic disease icon for the patient who has one or more familymembers assigned with a diagnosis indicating a genetic disease.
 8. Thecomputer-readable media of claim 7, further comprising receiving aninteraction with the probable genetic disease icon.
 9. Thecomputer-readable media of claim 8, further comprising, upon receivingthe interaction with the probable genetic disease icon, providing arelative name, relationship to the patient, and diagnosis.
 10. Thecomputer-readable media of claim 1, further comprising, upon receivingan indication that the one or more family members was misdiagnosed witha genetic disease, updating a record for the patient and correspondingfamily members in the healthcare system with no alerts indicating thepatient does not have a probable genetic disease and the correspondingfamily members do not have the genetic disease.
 11. Thecomputer-readable media of claim 1, further comprising, upon receivingan indication that the patient has been ruled out as having the geneticdisease, updating a record of the patient in the healthcare system withno alerts indicating the patient does not have a probable geneticdisease, including removing the probable genetic disease icon from theelectronic health record of the patient.
 12. A method for providing anindicator for probable inheritance of genetic disease, the methodcomprising: identifying, by a genetic disease engine, parents,grandparents, or siblings of a patient collected during registration ofthe patient at a clinician device; determining, at the genetic diseaseengine by communicating with one or more medical devices that provideinsight into whether the patient, the parents, grandparents, or siblingsof the patient been assigned with a diagnosis indicating a geneticdisease, that one of the patient or the parents, grandparents, orsiblings of the patient has been assigned with the diagnosis indicatingthe genetic disease; and upon determining that one of the patient or theparents, grandparents, or siblings of the patient has been assigned withthe diagnosis indicating the genetic disease, providing, by the geneticdisease engine, an alert for genetic disease or probable genetic diseasefor the patient or family member of the patient, the alert includingproviding a genetic disease icon or probable genetic disease icon in anelectronic health record of the patient or family member of the patient;communicating, by the genetic disease engine, orders that assist inconfirming or ruling out the patient having the disease; prompting aclinician, via the clinician device, to confirm or rule out the patienthaving the disease; and upon receiving an indication that the patient orfamily member has been confirmed as having the genetic disease,replacing the probable genetic disease icon with a genetic disease iconin the electronic health record of the patient or family memberindicating the patient or family member has the genetic disease.
 13. Themethod of claim 12, wherein the alert includes an option to assign thegenetic disease to the patient or other family members within thehealthcare system.
 14. The method of claim 13, further comprisingproviding a genetic disease icon for the one or more family members thathas been assigned with a genetic disease.
 15. The method of claim 14,further comprising receiving an interaction with the genetic diseaseicon.
 16. The method of claim 15, further comprising, upon receiving theinteraction with the genetic disease icon, providing a relative name,relationship to the patient, and diagnosis.
 17. The method of claim 12,further comprising providing a probable genetic disease icon for patientwho has one or more family members assigned with a diagnosis indicatinga genetic disease.
 18. The method of claim 17, further comprisingreceiving an interaction with the probable genetic disease icon.
 19. Themethod of claim 18, further comprising, upon receiving the interactionwith the probable genetic disease icon, providing a relative name,relationship to the patient, and diagnosis.
 20. The method of claim 12,further comprising, upon receiving an indication that the patient orfamily member has been ruled out as having the genetic disease, updatinga record of the patient or family member in the healthcare system withno alerts indicating the patient or family member does not have geneticdisease or probable genetic disease, including removing the geneticdisease icon or probable genetic disease icon from the electronic healthrecord of the patient or family member of the patient.
 21. A system in ahealthcare computing environment comprising: a processor; and anon-transitory computer storage medium storing computer-useableinstructions that, when used by the processor, causes the processor to:access, via a clinician device, a genetic disease engine to identifyparents, grandparents, or siblings of a patient collected duringregistration of the patient; determine, at the genetic disease engine bycommunicating with one or more medical devices that provide insight intowhether the patient, the parents, grandparents, or siblings of thepatient has been assigned with a diagnosis indicating a genetic disease,that one of the patient or the parents, grandparents, or siblings of thepatient has been assigned with the diagnosis indicating the geneticdisease; upon determining a family member of the one or more familymembers has been assigned with the diagnosis indicating the geneticdisease, provide, by the genetic disease engine, an alert for geneticdisease or probable genetic disease for the patient or family member ofthe patient; communicate, by the genetic disease engine, orders thatassist in confirming or ruling out the patient having the disease;prompt a clinician to confirm or rule out the patient or family memberhaving the disease; and upon receiving an indication that the patient orfamily member has been confirmed as having the genetic disease,replacing the probable genetic disease icon with a genetic disease iconin the electronic health record of the patient or family memberindicating the patient or family member has the genetic disease.